Please Wait
Applying Filters...
Menu
Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 1ALCOHOL

02 1CABERGOLINE

03 3CLONIDINE

04 1DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE

05 2IVABRADINE HYDROCHLORIDE

06 4LEVETIRACETAM

07 1LIFITEGRAST

08 1PANTOPRAZOLE SODIUM

09 1TAFLUPROST

10 2TIMOLOL MALEATE

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

Brand Name : DEHYDRATED ALCOHOL

COMPAMED
Not Confirmed
arrow

Brand Name : DEHYDRATED ALCOHOL

arrow
COMPAMED
Not Confirmed

Ingenus Pharmaceuticals

Dosage Form : SOLUTION;INTRA-ARTERIAL

Brand Name : DEHYDRATED ALCOHOL

Dosage Strength : 99% (5ML)

Packaging :

Approval Date : 2025-07-09

Application Number : 219569

Regulatory Info : RX

Registration Country : USA

blank

02

Brand Name : CABERGOLINE

COMPAMED
Not Confirmed
arrow

Brand Name : CABERGOLINE

arrow
COMPAMED
Not Confirmed

Ingenus Pharmaceuticals

Dosage Form : TABLET;ORAL

Brand Name : CABERGOLINE

Dosage Strength : 0.5MG

Packaging :

Approval Date : 2018-08-01

Application Number : 204735

Regulatory Info : RX

Registration Country : USA

blank

03

Brand Name : CLONIDINE

COMPAMED
Not Confirmed
arrow

Brand Name : CLONIDINE

arrow
COMPAMED
Not Confirmed

Ingenus Pharmaceuticals

Dosage Form : SYSTEM;TRANSDERMAL

Brand Name : CLONIDINE

Dosage Strength : 0.1MG/24HR

Packaging :

Approval Date : 2009-08-18

Application Number : 76157

Regulatory Info : RX

Registration Country : USA

blank

04

Brand Name : CLONIDINE

COMPAMED
Not Confirmed
arrow

Brand Name : CLONIDINE

arrow
COMPAMED
Not Confirmed

Ingenus Pharmaceuticals

Dosage Form : SYSTEM;TRANSDERMAL

Brand Name : CLONIDINE

Dosage Strength : 0.2MG/24HR

Packaging :

Approval Date : 2009-08-18

Application Number : 76157

Regulatory Info : RX

Registration Country : USA

blank

05

Brand Name : CLONIDINE

COMPAMED
Not Confirmed
arrow

Brand Name : CLONIDINE

arrow
COMPAMED
Not Confirmed

Ingenus Pharmaceuticals

Dosage Form : SYSTEM;TRANSDERMAL

Brand Name : CLONIDINE

Dosage Strength : 0.3MG/24HR

Packaging :

Approval Date : 2009-08-18

Application Number : 76157

Regulatory Info : RX

Registration Country : USA

blank

06

Brand Name : DORZOLAMIDE HYDROCHL...

COMPAMED
Not Confirmed
arrow

Brand Name : DORZOLAMIDE HYDROCHL...

arrow
COMPAMED
Not Confirmed

Ingenus Pharmaceuticals

Dosage Form : SOLUTION/DROPS;OPHTHALMI...

Brand Name : DORZOLAMIDE HYDROCHLORIDE...

Dosage Strength : EQ 2% BASE;EQ 0.5% BAS...

Packaging :

Approval Date : 2023-05-01

Application Number : 217260

Regulatory Info : RX

Registration Country : USA

blank

07

Brand Name : IVABRADINE HYDROCHLO...

COMPAMED
Not Confirmed
arrow

Brand Name : IVABRADINE HYDROCHLO...

arrow
COMPAMED
Not Confirmed

Ingenus Pharmaceuticals

Dosage Form : TABLET;ORAL

Brand Name : IVABRADINE HYDROCHLORIDE

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2021-12-30

Application Number : 214051

Regulatory Info : RX

Registration Country : USA

blank

08

Brand Name : IVABRADINE HYDROCHLO...

COMPAMED
Not Confirmed
arrow

Brand Name : IVABRADINE HYDROCHLO...

arrow
COMPAMED
Not Confirmed

Ingenus Pharmaceuticals

Dosage Form : TABLET;ORAL

Brand Name : IVABRADINE HYDROCHLORIDE

Dosage Strength : EQ 7.5MG BASE

Packaging :

Approval Date : 2021-12-30

Application Number : 214051

Regulatory Info : RX

Registration Country : USA

blank

09

Brand Name : LEVETIRACETAM

COMPAMED
Not Confirmed
arrow

Brand Name : LEVETIRACETAM

arrow
COMPAMED
Not Confirmed

Ingenus Pharmaceuticals

Dosage Form : TABLET;ORAL

Brand Name : LEVETIRACETAM

Dosage Strength : 250MG

Packaging :

Approval Date : 2009-01-15

Application Number : 79042

Regulatory Info : RX

Registration Country : USA

blank

10

Brand Name : LEVETIRACETAM

COMPAMED
Not Confirmed
arrow

Brand Name : LEVETIRACETAM

arrow
COMPAMED
Not Confirmed

Ingenus Pharmaceuticals

Dosage Form : TABLET;ORAL

Brand Name : LEVETIRACETAM

Dosage Strength : 500MG

Packaging :

Approval Date : 2009-01-15

Application Number : 79042

Regulatory Info : RX

Registration Country : USA

blank